Canonical Allele Identifier: CA1335317526

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232542997G= , CM000664.2:g.232542997G=	GRCh38
NC_000002.11:g.233407707G= , CM000664.1:g.233407707G=	GRCh37
NC_000002.10:g.233115951G=	NCBI36
NG_012954.1:g.8271G=
NG_012954.2:g.8306G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000651502.1:c.720G= MANE Select	ENSP00000498757.1:p.Lys240=
ENST00000389492.3:c.564G=	ENSP00000374143.3:p.Lys188=
ENST00000389494.7:c.720G=	ENSP00000374145.3:p.Lys240=
NM_005199.4:c.720G=	NP_005190.4:p.Lys240=
NM_005199.5:c.720G= MANE Select	NP_005190.4:p.Lys240=